Effect of Topical CBD Cream for Degenerative Hallux Disorders
Primary Purpose
Hallux Valgus, Hallux Rigidus
Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
magnesium-cannabidiolic acid cream
Placebo cream
Sponsored by
About this trial
This is an interventional treatment trial for Hallux Valgus
Eligibility Criteria
Inclusion Criteria:
- Patients with a new diagnosis of hallux rigidus or hallux valgus
- VAS pain score of 4 or higher
- Age > 18 years
- The patient provides informed consent
Exclusion Criteria:
- A previous operative procedure to the first metatarsal for treatment of hallux valgus or hallux rigidus
- VAS pain score at presentation less than 4
- Concomitant hallux valgus and hallux rigidus on the ipsilateral side
- Allergy to CBD, Cannabidiolic acid (CBDa) or any other ingredient contained in the topical cream
- Pregnant patients
Sites / Locations
- Midwest Orthopaedics at Rush
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
Mg-CBDa cream
Placebo cream
Arm Description
Subjects in this group will receive the active Mg-CBDa (magnesium-cannabidiolic acid) for topical treatment of hallux valgus or hallux rigidus.
Subjects in this group will receive the inactive CBD cream for topical treatment of hallux valgus or hallux rigidus. The ingredients of the placebo cream are: butyrospermum parkii (shea butter), caprylic/capric triglycerides medium-chain triglycerides (MCT oil), and food coloring to match the CBD oil. There will be 345 grams of shea butter and 62ml MCT oil per batch.
Outcomes
Primary Outcome Measures
Post-treatment VAS score averaged daily over 4 weeks.
Weekly visual analog system (VAS) pain scores will be measured daily for four weeks. The VAS pain score is a measure of pain severity. It is measured on a scale from 0 to 10, with 10 being the worst pain the patient has experienced.
Weekly Foot Function Index
The foot function index (FFI) is a questionnaire that measures foot pain and disability. It is self-administered and consists of 23 items divided into 3 subscales (pain, disability, and activity limitation). The pain subcategory consists of 9 questions (scored out of 90) and is a measure of pain in different situations, such as walking with shoes versus barefoot. The disability subcategory consists of 9 questions (scored out of 90) and measures functional activities, such as difficulty walking upstairs. The activity limitation subcategory consists of 5 questions (scored out of 50) and measures limitations caused by the foot problem. All three subcategories are summed together to get a final number, with higher numbers indicating worse pain.
Secondary Outcome Measures
Full Information
NCT ID
NCT04103814
First Posted
September 23, 2019
Last Updated
May 15, 2023
Sponsor
Rush University Medical Center
Collaborators
Mid-America Orthopaedic Association (MAOA)
1. Study Identification
Unique Protocol Identification Number
NCT04103814
Brief Title
Effect of Topical CBD Cream for Degenerative Hallux Disorders
Official Title
Effect of Topical CBD Oil on Pain Scores for Hallux Disorders: A Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
May 2023
Overall Recruitment Status
Terminated
Why Stopped
Lack of resources to continue enrollment
Study Start Date
October 20, 2019 (Actual)
Primary Completion Date
May 15, 2023 (Actual)
Study Completion Date
May 15, 2023 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Rush University Medical Center
Collaborators
Mid-America Orthopaedic Association (MAOA)
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
5. Study Description
Brief Summary
Hallux rigidus and hallux valgus are chronic forefoot conditions associated with pain, inflammation and functional impairment. Topical cannabidiol (CBD) cream has been shown to decrease inflammation, swelling, and pain response in arthritis models with minimal side effects, although the intervention has never been studied in hallux valgus or hallux rigidus. The purpose of this study is to determine if topical CBD cream is an effective treatment for pain secondary to hallux rigidus and hallux valgus.
Detailed Description
Hallux rigidus and hallux valgus are chronic forefoot conditions associated with pain, inflammation and functional impairment. While operative interventions exist, nonoperative modalities are the mainstay of treatment for most patients. Options include shoe wear modification, manual and physical therapy, intraarticular injection of corticosteroids or sodium hyaluronate, oral nonsteroidal anti-inflammatories, and foot orthoses. Oral anti-inflammatories are the most effective non-operative strategy, but unfortunately, are associated with major adverse side effects and are contraindicated in many patients. Topical cannabidiol (CBD) cream has been shown to decrease inflammation, swelling, and pain response in arthritis models with minimal side effects, although the intervention has never been studied in hallux valgus or hallux rigidus. This prospective randomized trial will compare topical CBD cream vs placebo cream for the treatment of pain secondary to hallux valgus and hallux rigidus. The primary outcome of interest in the change in pre and post-treatment Visual Analog System (VAS) pain scores. VAS pain score is a measurement on a continuum of values of pain intensity. The purpose of this study is to determine if topical CBD cream is an effective treatment for pain secondary to hallux rigidus and hallux valgus.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hallux Valgus, Hallux Rigidus
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Model Description
Enrolled patients will receive either active Mg-CBDa (magnesium-cannabidiolic acid) cream or placebo cream (neutral emollient containing no active agent) for topical treatment of hallux rigidus or hallux valgus.
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
11 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Mg-CBDa cream
Arm Type
Active Comparator
Arm Description
Subjects in this group will receive the active Mg-CBDa (magnesium-cannabidiolic acid) for topical treatment of hallux valgus or hallux rigidus.
Arm Title
Placebo cream
Arm Type
Placebo Comparator
Arm Description
Subjects in this group will receive the inactive CBD cream for topical treatment of hallux valgus or hallux rigidus. The ingredients of the placebo cream are: butyrospermum parkii (shea butter), caprylic/capric triglycerides medium-chain triglycerides (MCT oil), and food coloring to match the CBD oil. There will be 345 grams of shea butter and 62ml MCT oil per batch.
Intervention Type
Drug
Intervention Name(s)
magnesium-cannabidiolic acid cream
Intervention Description
Patients will receive Mg-CBDa (magnesium-cannabidiolic acid) cream for topical treatment of hallux rigidus or hallux valgus.
Intervention Type
Drug
Intervention Name(s)
Placebo cream
Intervention Description
Patients will receive placebo cream (neutral emollient containing no active agent) for topical treatment of hallux rigidus or hallux valgus. The ingredients of the placebo cream are as follows: Butyrospermum parkii (shea butter), caprylic/capric triglycerides medium-chain triglycerides (MCT oil), food coloring to match the CBD oil. There will be 345 grams of shea butter and 62ml MCT oil per batch.
Primary Outcome Measure Information:
Title
Post-treatment VAS score averaged daily over 4 weeks.
Description
Weekly visual analog system (VAS) pain scores will be measured daily for four weeks. The VAS pain score is a measure of pain severity. It is measured on a scale from 0 to 10, with 10 being the worst pain the patient has experienced.
Time Frame
4 weeks
Title
Weekly Foot Function Index
Description
The foot function index (FFI) is a questionnaire that measures foot pain and disability. It is self-administered and consists of 23 items divided into 3 subscales (pain, disability, and activity limitation). The pain subcategory consists of 9 questions (scored out of 90) and is a measure of pain in different situations, such as walking with shoes versus barefoot. The disability subcategory consists of 9 questions (scored out of 90) and measures functional activities, such as difficulty walking upstairs. The activity limitation subcategory consists of 5 questions (scored out of 50) and measures limitations caused by the foot problem. All three subcategories are summed together to get a final number, with higher numbers indicating worse pain.
Time Frame
4 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with a new diagnosis of hallux rigidus or hallux valgus
VAS pain score of 4 or higher
Age > 18 years
The patient provides informed consent
Exclusion Criteria:
A previous operative procedure to the first metatarsal for treatment of hallux valgus or hallux rigidus
VAS pain score at presentation less than 4
Concomitant hallux valgus and hallux rigidus on the ipsilateral side
Allergy to CBD, Cannabidiolic acid (CBDa) or any other ingredient contained in the topical cream
Pregnant patients
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Simon Lee, MD
Organizational Affiliation
Midwest Orthopaedics at Rush
Official's Role
Principal Investigator
Facility Information:
Facility Name
Midwest Orthopaedics at Rush
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60612
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Effect of Topical CBD Cream for Degenerative Hallux Disorders
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